Zhang Nicole K, Zhang Selena K, Zhang Li I, Tao Huizhong W, Zhang Guang-Wei
Zilkha Neurogenetic Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA, United States.
Biomedical Engineering Program, Viterbi School of Engineering, University of Southern California, Los Angeles, CA, United States.
Front Aging Neurosci. 2023 Aug 15;15:1213379. doi: 10.3389/fnagi.2023.1213379. eCollection 2023.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder primarily affecting cognitive functions. However, sensory deficits in AD start to draw attention due to their high prevalence and early onsets which suggest that they could potentially serve as diagnostic biomarkers and even contribute to the disease progression. This literature review examines the sensory deficits and cortical pathological changes observed in visual, auditory, olfactory, and somatosensory systems in AD patients, as well as in various AD animal models. Sensory deficits may emerge at the early stages of AD, or even precede the cognitive decline, which is accompanied by cortical pathological changes including amyloid-beta deposition, tauopathy, gliosis, and alterations in neuronal excitability, synaptic inputs, and functional plasticity. Notably, these changes are more pronounced in sensory association areas and superficial cortical layers, which may explain the relative preservation of basic sensory functions but early display of deficits of higher sensory functions. We propose that sensory impairment and the progression of AD may establish a cyclical relationship that mutually perpetuates each condition. This review highlights the significance of sensory deficits with or without cortical pathological changes in AD and emphasizes the need for further research to develop reliable early detection and intervention through sensory systems.
阿尔茨海默病(AD)是一种主要影响认知功能的进行性神经退行性疾病。然而,AD中的感觉缺陷因其高患病率和早期发病而开始受到关注,这表明它们有可能作为诊断生物标志物,甚至对疾病进展产生影响。这篇文献综述研究了AD患者以及各种AD动物模型在视觉、听觉、嗅觉和躯体感觉系统中观察到的感觉缺陷和皮质病理变化。感觉缺陷可能在AD的早期出现,甚至先于认知能力下降,同时伴有皮质病理变化,包括β-淀粉样蛋白沉积、tau病变、神经胶质增生以及神经元兴奋性、突触输入和功能可塑性的改变。值得注意的是,这些变化在感觉联合区和皮质浅层更为明显,这可能解释了基本感觉功能相对保留但高级感觉功能缺陷早期出现的原因。我们提出,感觉障碍与AD的进展可能建立一种相互促进的循环关系。这篇综述强调了AD中伴有或不伴有皮质病理变化的感觉缺陷的重要性,并强调需要进一步研究,以通过感觉系统开发可靠的早期检测和干预方法。